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Amyotrophic Lateral Sclerosis
Hierarchy: | ∟ ∟ ∟ ∟ Amyotrophic Lateral Sclerosis 14 coordinate concepts∟ ∟ ∟ ∟ Amyotrophic Lateral Sclerosis 14 coordinate concepts∟ ∟ ∟ ∟ Amyotrophic Lateral Sclerosis 14 coordinate conceptsX |
Broader terms: | ∟ ∟ ∟ ∟ Amyotrophic Lateral Sclerosis ∟ ∟ ∟ ∟ Amyotrophic Lateral Sclerosis ∟ ∟ ∟ ∟ Amyotrophic Lateral Sclerosis |
Scope note: | A degenerative disorder affecting upper MOTOR NEURONS in the brain and lower motor neurons in the brain stem and SPINAL CORD. Disease onset is usually after the age of 50 and the process is usually fatal within 3 to 6 years. Clinical manifestations include progressive weakness, atrophy, FASCICULATION, hyperreflexia, DYSARTHRIA, dysphagia, and eventual paralysis of respiratory function. Pathologic features include the replacement of motor neurons with fibrous ASTROCYTES and atrophy of anterior SPINAL NERVE ROOTS and corticospinal tracts. (From Adams et al., Principles of Neurology, 6th ed, pp1089-94)
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activeMeSHYear*: | |
dateCreated*: | 1999-01-01X |
dateRevised*: | 2002-07-02X |
recordAuthorizer*: | sjnX |
recordMaintainer*: | mdbX |
recordOriginator*: | NLMX |
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Labels and equivalent concepts: | Amyotrofinen lateraaliskleroosi (fi) XALS (fi, replaced) Liikeratakovettumatauti (fi, replaced) Amyotrofisk lateralskleros (sv) ALS (sv, replaced) Motor Neuron Disease, Amyotrophic Lateral Sclerosis (en, replaced) Lou Gehrig's Disease (en, replaced) Dementia With Amyotrophic Lateral Sclerosis (en, replaced) Gehrig's Disease (en, replaced) Guam Form of Amyotrophic Lateral Sclerosis (en, replaced) Lou Gehrig Disease (en, replaced) ALS (Amyotrophic Lateral Sclerosis) (en, replaced) Sclerosis lateralis amyotrophica (la-FI, replaced) |
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